Cytosolic pH Regulates Cell Growth through Distinct GTPases, Arf1 and Gtr1, to Promote Ras/PKA and TORC1 Activity

被引:97
作者
Dechant, Reinhard [1 ,2 ]
Saad, Shady [1 ,3 ]
Ibanez, Alfredo J. [4 ]
Peter, Matthias [1 ,2 ]
机构
[1] ETH, Inst Biochem, CH-8093 Zurich, Switzerland
[2] Competence Ctr Syst Physiol & Metab Dis, CH-8093 Zurich, Switzerland
[3] Life Sci Zurich, PhD Program Syst Biol Complex Dis, CH-8093 Zurich, Switzerland
[4] ETH, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
VACUOLAR H+-ATPASE; TRANSFER-RNA SYNTHETASE; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTION FACTORS; NUCLEAR-LOCALIZATION; RAG GTPASES; AMINO-ACIDS; EGO COMPLEX; YEAST; PROTEIN;
D O I
10.1016/j.molcel.2014.06.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regulation of cell growth by nutrients is governed by highly conserved signaling pathways, yet mechanisms of nutrient sensing are still poorly understood. In yeast, glucose activates both the Ras/PKA pathway and TORC1, which coordinately regulate growth through enhancing translation and ribosome biogenesis and suppressing autophagy. Here, we show that cytosolic pH acts as a cellular signal to activate Ras and TORC1 in response to glucose availability. We demonstrate that cytosolic pH is sensitive to the quality and quantity of the available carbon source (C-source). Interestingly, Ras/PKA and TORC1 are both activated through the vacuolar ATPase (V-ATPase), which was previously identified as a sensor for cytosolic pH in vivo. V-ATPase interacts with two distinct GTPases, Arf1 and Gtr1, which are required for Ras and TORC1 activation, respectively. Together, these data provide a molecular mechanism for how cytosolic pH links C-source availability to the activity of signaling networks promoting cell growth.
引用
收藏
页码:409 / 421
页数:13
相关论文
共 52 条
[1]   The TOR signalling pathway controls nuclear localization of nutrient-regulated transcription factors [J].
Beck, T ;
Hall, MN .
NATURE, 1999, 402 (6762) :689-692
[2]   The Vam6 GEF Controls TORC1 by Activating the EGO Complex [J].
Binda, Matteo ;
Peli-Gulli, Marie-Pierre ;
Bonfils, Gregory ;
Panchaud, Nicolas ;
Urban, Joerg ;
Sturgill, Thomas W. ;
Loewith, Robbie ;
De Virgilio, Claudio .
MOLECULAR CELL, 2009, 35 (05) :563-573
[3]   ARF PROTEINS - THE MEMBRANE TRAFFIC POLICE [J].
BOMAN, AL ;
KAHN, RA .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (04) :147-150
[4]   Leucyl-tRNA Synthetase Controls TORC1 via the EGO Complex [J].
Bonfils, Gregory ;
Jaquenoud, Malika ;
Bontron, Severine ;
Ostrowicz, Clemens ;
Ungermann, Christian ;
De Virgilio, Claudio .
MOLECULAR CELL, 2012, 46 (01) :105-110
[5]   Nutritional Control of Growth and Development in Yeast [J].
Broach, James R. .
GENETICS, 2012, 192 (01) :73-105
[6]   REPLACEMENT OF THE PROMOTER OF THE YEAST PLASMA-MEMBRANE ATPASE GENE BY A GALACTOSE-DEPENDENT PROMOTER AND ITS PHYSIOLOGICAL CONSEQUENCES [J].
CID, A ;
PERONA, R ;
SERRANO, R .
CURRENT GENETICS, 1987, 12 (02) :105-110
[7]   Rb, whi it's not just for metazoans anymore [J].
Cooper, K. .
ONCOGENE, 2006, 25 (38) :5228-5232
[8]   Requirement of Prorenin Receptor and Vacuolar H+-ATPase-Mediated Acidification for Wnt Signaling [J].
Cruciat, Cristina-Maria ;
Ohkawara, Bisei ;
Acebron, Sergio P. ;
Karaulanov, Emil ;
Reinhard, Carmen ;
Ingelfinger, Dierk ;
Boutros, Michael ;
Niehrs, Christof .
SCIENCE, 2010, 327 (5964) :459-463
[9]   The mTORC1 Pathway Stimulates Glutamine Metabolism and Cell Proliferation by Repressing SIRT4 [J].
Csibi, Alfred ;
Fendt, Sarah-Maria ;
Li, Chenggang ;
Poulogiannis, George ;
Choo, Andrew Y. ;
Chapski, Douglas J. ;
Jeong, Seung Min ;
Dempsey, Jamie M. ;
Parkhitko, Andrey ;
Morrison, Tasha ;
Henske, Elizabeth P. ;
Haigis, Marcia C. ;
Cantley, Lewis C. ;
Stephanopoulos, Gregory ;
Yu, Jane ;
Blenis, John .
CELL, 2013, 153 (04) :840-854
[10]   The N-terminal domain of the V-ATPase subunit 'a' is regulated by pH in vitro and in vivo [J].
Dechant, Reinhard ;
Peter, Matthias .
CHANNELS, 2011, 5 (01) :4-8